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    Congenital Nephrotic Syndrome: Case Report and Review of Literature
    (Cukurova Univ, Fac Medicine, 2012) Konak, Murat; Annagur, Ali; Altunhan, H.; Atas, Bulent; Ors, Rahmi
    Congenital nephrotic syndrome (CNS) is a rare kidney disease which reveals itself after birth and characterized with severe proteinuria, hypoalbuminemia and edema. It is a genetic disorder that occurs with deterioration of glomerular filtration barrier especially as a result of mutation that develops in genes called nephrin and podocin. CNS could be as a result of perinatal infection as well as a part of a genetic syndrome. Immune suppressive treatment is ineffective in genetically originated CNS, however renal transplantation yields curative treatment. In many cases to prevent from life threatening edema, daily albumin infusion is needed. Additionally, high caloric diet, thyroxin and mineral supply are applied. Also prophylaxis of thrombolytic complications and opportunistic infection that could develop due to immune deficiency is needed. In this report we discussed a case with the review of literature by reporting a newborn which had CNS diagnosis as a result of persistent hypoalbuminemia and proteinuria without edema.
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    Prenatal diagnosis of ring chromosome 4 and Wolf-Hirschorn syndrome with bilateral polycystic kidney disease
    (Nature Publishing Group, 2019) Tasdemir, P.; Gultekin, N. D.; Ercan, F.; Yilmaz, F. H.; Acar, A.; Altunhan, H.
    [Abstract Not Availabe]